Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?

Background. Elevated levels of soluble CD40 Ligand (sCD40L) were found in serum but not in plasma of patients with chronic spontaneous urticaria (CU). What is important is that sCD40L has proinflammatory properties, and its elevated plasma level may indicate increased risk of cardiovascular events....

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Main Authors: T. Jasinska, A. Grzanka, E. Machura, A. Kasperska-Zajac
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2013/823798
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spelling doaj-381adf288ec6442bb14f1c0eb22361242020-11-24T23:25:43ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/823798823798Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?T. Jasinska0A. Grzanka1E. Machura2A. Kasperska-Zajac3Chair and Clinical Department of Internal Diseases, Dermatology and Allergology ul. M. Curie-Skłodowskiej 10, Medical University of Silesia in Katowice, 41-800 Zabrze, PolandChair and Clinical Department of Internal Diseases, Dermatology and Allergology ul. M. Curie-Skłodowskiej 10, Medical University of Silesia in Katowice, 41-800 Zabrze, PolandDepartment of Pediatric in Zabrze, Medical University of Silesia, PolandChair and Clinical Department of Internal Diseases, Dermatology and Allergology ul. M. Curie-Skłodowskiej 10, Medical University of Silesia in Katowice, 41-800 Zabrze, PolandBackground. Elevated levels of soluble CD40 Ligand (sCD40L) were found in serum but not in plasma of patients with chronic spontaneous urticaria (CU). What is important is that sCD40L has proinflammatory properties, and its elevated plasma level may indicate increased risk of cardiovascular events. These observations should stimulate further evaluation of sCD40L in different forms of urticaria. Aim. In the present study, sCD40L plasma level was investigated in delayed pressure urticaria (DPU). Methods. As platelets are predominant and variable sources of sCD40L, we investigated sCD40L concentration in platelet-poor plasma (PPP), which seems the best way to minimize the potential contribution of these cells to the ligand level. Results. Plasma sCD40L concentration was significantly increased in the DPU group compared to the healthy controls. Conclusions. It seems that DPU is associated with increased systemic release of sCD40L, which is believed to derive predominantly from activated platelets. The present study as well as the earlier contributions suggest that distinct cells activity, including platelets, may be identified in different types of urticaria.http://dx.doi.org/10.1155/2013/823798
collection DOAJ
language English
format Article
sources DOAJ
author T. Jasinska
A. Grzanka
E. Machura
A. Kasperska-Zajac
spellingShingle T. Jasinska
A. Grzanka
E. Machura
A. Kasperska-Zajac
Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?
BioMed Research International
author_facet T. Jasinska
A. Grzanka
E. Machura
A. Kasperska-Zajac
author_sort T. Jasinska
title Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?
title_short Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?
title_full Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?
title_fullStr Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?
title_full_unstemmed Is Delayed Pressure Urticaria Associated with Increased Systemic Release of sCD40L?
title_sort is delayed pressure urticaria associated with increased systemic release of scd40l?
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2013-01-01
description Background. Elevated levels of soluble CD40 Ligand (sCD40L) were found in serum but not in plasma of patients with chronic spontaneous urticaria (CU). What is important is that sCD40L has proinflammatory properties, and its elevated plasma level may indicate increased risk of cardiovascular events. These observations should stimulate further evaluation of sCD40L in different forms of urticaria. Aim. In the present study, sCD40L plasma level was investigated in delayed pressure urticaria (DPU). Methods. As platelets are predominant and variable sources of sCD40L, we investigated sCD40L concentration in platelet-poor plasma (PPP), which seems the best way to minimize the potential contribution of these cells to the ligand level. Results. Plasma sCD40L concentration was significantly increased in the DPU group compared to the healthy controls. Conclusions. It seems that DPU is associated with increased systemic release of sCD40L, which is believed to derive predominantly from activated platelets. The present study as well as the earlier contributions suggest that distinct cells activity, including platelets, may be identified in different types of urticaria.
url http://dx.doi.org/10.1155/2013/823798
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